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SLEEP 2011 Abstract Supplement

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B. Clinical Sleep Science VII. Neurological Disorders and Sleep<br />

headache over one year’s time were analyzed. As a part of their evaluation,<br />

those patients were queried regarding their sleep, and, if appropriate,<br />

were studied with polysomnography in an accredited sleep disorders<br />

center. Patients with changes on the neurologic exam suggestive of cervical<br />

radiculopathy were examined with EMG-NCV testing.<br />

Results: Of the 700 patients who had a diagnosis of headache on initial<br />

evaluation, 491 (70%) also had sleep diagnoses. Of these patients with<br />

sleep diagnoses, 277 (56%) completed polysomnography examinations.<br />

76% of the polysomnography group had upper airway resistance syndrome<br />

(UARS) or obstructive sleep apnea (OSA). Striking in the polysomnography<br />

group patients was the presence of concomitant cervical<br />

radiculopathy (73 %). Of the patients with cervical radiculopathy, 50%<br />

or more of total sleep time was spent in non-supine sleep, despite request<br />

by the technologist to sleep supine.<br />

Conclusion: 1. Headache is strongly associated with sleep disordered<br />

breathing. 2. Cervical radiculopathy is strongly associated with sleep<br />

disordered breathing, confirming a previous study. 3. Non-supine sleep<br />

provoked by sleep disordered breathing may play a previously unrecognized<br />

role in headache and cervical radiculopathy.<br />

0633<br />

SEIZURE REDUCTION FOLLOWING NASAL CONTINUOUS<br />

POSITIVE AIRWAY PRESSURE THERAPY FOR CO-MORBID<br />

OBSTRUCTIVE <strong>SLEEP</strong> APNEA IN EPILEPSY<br />

St. Louis EK 1 , Berth W 2 , Zimmerman B 3 , Dyken ME 2 , Granner MA 2<br />

1<br />

Department of Neurology, Mayo Clinic, Rochester, MN, USA,<br />

2<br />

Department of Neurology, University of Iowa Hospitals and Clinics,<br />

Iowa City, IA, USA, 3 Department of Biostatistics, University of Iowa<br />

College of Public Health, Iowa City, IA, USA<br />

Introduction: Co-morbid OSA is frequent in epilepsy, and treatment<br />

with nCPAP may reduce seizure frequency but the degree of impact on<br />

seizure outcomes remains unclear. We hypothesized that seizure frequency<br />

would be reduced by nasal continuous positive airway pressure<br />

(nCPAP) therapy in epilepsy patients with co-morbid obstructive sleep<br />

apnea (OSA). We aimed to analyze the impact of nCPAP therapy on<br />

seizure frequency.<br />

Methods: We retrospectively analyzed 184 epilepsy patients who underwent<br />

polysomnography between 1/1/00-5/30/09. Demographic,<br />

seizure frequency, antiepileptic drug load, and PSG variables were recorded.<br />

Seizure frequency was compared between epilepsy patients with<br />

OSA (apnea-hypopnea index (AHI)>5/hour) who were compliant with<br />

nCPAP and those who either deferred nCPAP or were non-compliant.<br />

Group comparisons were analyzed with 2-tailed T-tests or Wilcoxon<br />

signed rank tests in JMP or SAS (Chicago, IL).<br />

Results: 110 (60%) epilepsy patients had OSA. Average AHI was 22.4<br />

± 20.8. Forty-three patients received nCPAP. Of 33 patients having<br />

pre- and post-nCPAP data, seizure frequency decreased significantly<br />

(t=2.138, p=0.04). 79% reported seizure reduction and 61% were responders<br />

(having a 50% or greater seizure reduction), and this effect held<br />

when antiepileptic drugs were unchanged or reduced (n=18, p=0.01). In<br />

patients who did not receive or comply with nCPAP therapy, there was<br />

no significant difference in seizure frequency (n=28, t=-1.411, p=0.17).<br />

Conclusion: nCPAP treatment significantly reduces seizure frequency,<br />

and the degree of seizure improvement appears comparable to the effect<br />

of adjunctive antiepileptic drug therapy. Further prospective studies of<br />

the impact of co-morbid OSA in epilepsy patients on seizure burden and<br />

interictal state factors crucial to quality of life (i.e., mood state, vulnerability<br />

to antiepileptic drug adverse effects, and sleepiness/vigilance) are<br />

warranted.<br />

Support (If Any): University of Iowa Carver College of Medicine<br />

Medical Student Summer Research Award; Mentored Clinical Research<br />

Scholar Program at Iowa (K12 RR017700-05); Grant Number<br />

1 UL1RR024150 from the National Center for Research Resources<br />

(NCRR)<br />

0634<br />

VAGUS NERVE STIMULATION THERAPY ENHANCES<br />

OBSTRUCTIVE RESPIRATIONS DURING <strong>SLEEP</strong><br />

Simmons JH 1,2 , Barlow S 1,2<br />

1<br />

Sadler Clinic Sleep Disorders Center, The Woodlands, TX, USA,<br />

2<br />

CSMA, Houston, TX, USA<br />

Introduction: Vagus Nerve Stimulator (VNS) therapy has been used in<br />

medication resistant Epilepsy with improved outcomes and utilization<br />

has increased over the past decade. In our center we have OSA patients<br />

with epilepsy that have VNS devices and have recognized many of these<br />

patients have periodic obstructive breathing patterns that correspond to<br />

their VNS stimulation settings. We sought to confirm this association<br />

and to also determine optimal methods of treating both the patients seizures<br />

and OSA rather than one at the detriment of the other.<br />

Methods: The study was done in two parts. First, we reviewed all of<br />

our patients who have both VNS devices for the treatment of their epilepsy<br />

and who underwent NPSG testing. Next, assessment was done to<br />

identify if there was an association between the VNS stimulation pattern<br />

and the occurrence of OSA. In one patient modifications were made in<br />

the VNS settings during NPSG testing to clearly confirm the association<br />

between VNS stimulation and OSA occurrence and then modifications<br />

were made on the VNS stimulation settings to identify parameters that<br />

stopped producing OSA.<br />

Results: Eight patients met our criteria of which six demonstrated OSA.<br />

All six demonstrated OSA in a pattern that correlated to the VNS stimulation<br />

rate. PAP titration was performed and initially prevented OSA<br />

from occurring during sleep. In three patients over time OSA worsened.<br />

Repeat titrations were performed and a clear pattern of periodic OSA<br />

was identified that was not adequately treated by prior CPAP pressures.<br />

To address the above observation one patient thus far was further<br />

evaluated by a repeat PAP titration. During the study, clear periodic obstructive<br />

apneas again occurred in accordance with her VNS settings.<br />

Stimulator parameters were modified to identify parameters that would<br />

not precipitate OSA. Lowering the stimulation rate from 25Hz down to<br />

10 Hz resolved the precipitation of OSA during the study.<br />

Conclusion: We claim that OSA is a potential complication of VNS<br />

therapy. This can be managed adequately but must be recognized when<br />

present. VNS stimulation parameters may require modification to optimize<br />

OSA treatment. We will present the clinical significance of these<br />

findings in relation to treating both OSA and Epilepsy. Further study is<br />

clearly needed on this topic since VNS is a useful treatment in Epilepsy<br />

patients.<br />

0635<br />

NOCTURNAL SEIZURES AND DYSREGULATION IN THE<br />

AUTONOMIC NERVOUS SYSTEM<br />

Kawai M 1 , Thapalia U 1 , Ohki N 2 , Verma A 1<br />

1<br />

Neurology/Neurophysiology, Neurological Institute, The Methodist<br />

Hospital, Houston, TX, USA, 2 NoruPro Light Systems, , Kokubunnji<br />

city, Japan<br />

Introduction: There are several reports that nocturnal seizures and sudden<br />

unexpected death in epileptic patients (SUDEP) is related. Correlation<br />

of autonomic nervous system (ANS) dysregulation and SUDEP<br />

has been recognized. Heart rate variability (HRV) has been utilized to<br />

evaluate ANS. High frequency (HF) component (0.15-0.4 Hz) of HRV<br />

is known to represent parasympathetic modulation. HF tends to appear<br />

steadily in normal NREM sleep. Temporal correlation between ANS and<br />

nocturnal seizure is not known well. Complex demodulation analysis of<br />

HRV allows us to detect dynamic changes in HF with temporal resolution<br />

of 6.25 seconds, whereas other analyses (i.e. fast Fourier transform)<br />

have that of 1-2 minutes.<br />

Methods: All of the nocturnal seizures captured in our epilepsy monitoring<br />

unit from January 2008 to September 2010 were reviewed retrospectively.<br />

Electrocardiogram data were analyzed with complex<br />

A219<br />

<strong>SLEEP</strong>, Volume 34, <strong>Abstract</strong> <strong>Supplement</strong>, <strong>2011</strong>

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